Elizabeth’s story – Maggie’s helped me to think ‘Yes, I can’
Police Officer Elizabeth had little contact from her hospital team during treatment due to the pandemic. It led to a very isolating period, made worse by lockdown restrictions. Maggie’s enabled Elizabeth to navigate a way ahead in the time she needed.
Jane’s story - I wouldn’t have come into the centre if it wasn’t for Tim
Jane and Tim were supported by Maggie's in Yorkshire when Tim's treatment was stopped due to coronavirus. We were able to support them both through the challenges they faced, with diagnosis, a pandemic, changing treatment and loss.
Lisa's story – from visitor to fundraiser
When I finished treatment for cancer, Maggie's was a huge support. I became determined to raise money.
Pete on the importance of sharing experiences
When I finished treatment for head and neck cancer I wanted to give something back. I worked with Maggie's to bring back the Heads2gether support group.
Dan's story - I was told I would never walk again
I was determined to get stronger against the odds, and Maggie's has helped me achieve that.
Laura's story – Maggie's helped me in my darkest moments
During treatment I would have been lost without Maggie's, so I decided to sign up for the Great North Run.
Tom's story – Maggie's gave us financial breathing space
I turned to Maggie's when my partner Thena was diagnosed with cancer because we didn't know how we'd pay her rent.
Christine's story – the support group was invaluable
When my doctor told me to join the head and neck cancer support group at Maggie's, I didn't think it would be for me. I couldn't have been more wrong.
Jim's story – finding strength in my support group
Getting over treatment for mouth cancer was tough. My Maggie's support group really helped.
Duncan's story – Maggie's was our second home
My wife Helen found a lump in her breast when our daughters were just 18 months and 5 years old. She was determined our whole family would have somewhere to go for support, and Maggie’s Edinburgh became a second home to us all.
Willie's story – mindfulness for mental health
I was at an all time low after treatment for prostate cancer but I joined a mindfulness course at Maggie's and made great friends.
Christian's story – organising a funeral during coronavirus
The plans for Grant’s funeral were overturned by social distancing. But Christian still found a fitting way for friends and family to honour his partner.
Lynn's story – support for siblings living in opposite ends of the country
Maggie’s supported siblings, Lynn and Grant at different centres in different ends of the country.
Alison on life with cancer, not dominated by cancer
It’s been an ‘interesting’ eighteen months in my life since May 2022 when, having lived 60 years as a healthy energetic & outgoing person, I was taken unwell completely out of the blue and diagnosed with ovarian cancer.
Marcus on talking to other men at Maggie's
My diagnosis was a shock. No one seemed to be concerned about my symptoms, not my GP, nor my consultant. Then suddenly I was diagnosed with incurable prostate cancer.
Alex on 'support for your support network' and running the London marathon
Alex was 33 years old and working as an Army Officer when he was diagnosed with stage 4 testicular cancer. He talks about how Maggie's supports his family and what running the London Marathon means to him.
Mary on concentrating on living thanks to Maggie's
After the shock of finding out her cancer was back, Mary put one foot in front of the other to complete the Camino de Santiago and start living her life to the full.
Viv and Ian on support every step of the way
When I got my original breast cancer diagnosis, I was told that I would only need a lumpectomy, radiotherapy and tablets. And I felt kind of ok about that. But then things changed in the autumn, the diagnosis changed to grade three.
Chris on finding a group that felt tailor-made for him
I started having investigations in April 2022 – an ultrasound, then an urgent CT scan. I was told I had a sinister growth on my pancreas. I knew exactly what that meant.
Liz on coming to Maggie’s every week
In 2015, my husband Dave was diagnosed with multiple myeloma. Since then he’s had numerous courses of chemotherapy and a stem cell transplant. He is on permanent chemotherapy that he has every day through a port.